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神经影像学和生物流体生物标志物在认知谱中老年人群体中的种族和民族差异。

Neuroimaging and biofluid biomarkers across race and ethnicity in older adults across the spectrum of cognition.

机构信息

1Florida Alzheimer's Disease Research Center (ADRC), University of Florida, Gainesville, FL, USA; Department of Applied Physiology and Kinesiology, University of Florida, Gainesville, FL, USA.

1Florida Alzheimer's Disease Research Center (ADRC), University of Florida, Gainesville, FL, USA; Department of Clinical and Health Psychology, University of Florida, Gainesville, FL, USA.

出版信息

Ageing Res Rev. 2024 Nov;101:102507. doi: 10.1016/j.arr.2024.102507. Epub 2024 Sep 19.

Abstract

Neuroimaging and biofluid biomarkers provide a proxy of pathological changes for Alzheimer's disease (AD) and are useful in improving diagnosis and assessing disease progression. However, it is not clear how race/ethnicity and different prevalence of AD risks impact biomarker levels. In this narrative review, we survey studies focusing on comparing biomarker differences between non-Hispanic White American(s) (NHW), African American(s) (AA), Hispanic/Latino American(s) (HLA), and Asian American(s) with normal cognition, mild cognitive impairment, and dementia. We found no strong evidence of racial and ethnic differences in imaging biomarkers after controlling for cognitive status and cardiovascular risks. For biofluid biomarkers, in AA, higher levels of plasma Aβ42/Aβ40, and lower levels of CSF total tau and p-tau 181, were observed after controlling for APOE status and comorbidities compared to NHW. Examining the impact of AD risks and comorbidities on biomarkers and their contributions to racial/ethnic differences in cognitive impairment are critical to interpreting biomarkers, understanding their generalizability, and eliminating racial/ethnic health disparities.

摘要

神经影像学和生物流体生物标志物为阿尔茨海默病 (AD) 的病理变化提供了替代指标,有助于改善诊断和评估疾病进展。然而,种族/民族和 AD 风险的不同流行率如何影响生物标志物水平尚不清楚。在本综述中,我们调查了专注于比较非西班牙裔白人 (NHW)、非裔美国人 (AA)、西班牙裔/拉丁裔 (HLA) 和亚裔美国人认知正常、轻度认知障碍和痴呆患者之间生物标志物差异的研究。我们发现,在控制认知状态和心血管风险后,影像学生物标志物没有明显的种族和民族差异。对于生物流体生物标志物,在 AA 中,与 NHW 相比,在控制 APOE 状态和合并症后,血浆 Aβ42/Aβ40 水平较高,CSF 总 tau 和 p-tau181 水平较低。检查 AD 风险和合并症对生物标志物的影响及其对认知障碍中种族/民族差异的贡献,对于解释生物标志物、理解其普遍性以及消除种族/民族健康差异至关重要。

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